| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28939675 | 0.882 | 0.200 | 22 | 19763273 | missense variant | T/A | snv | 3 | |||
| rs749275495 | 0.882 | 0.120 | 22 | 19764273 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 3 | |
| rs1274480565 | 0.925 | 0.120 | 22 | 19761154 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs1978060 | 0.925 | 0.040 | 22 | 19762002 | intron variant | A/G | snv | 0.64 | 2 | ||
| rs2238776 | 1.000 | 0.080 | 22 | 19770369 | intron variant | G/A;T | snv | 2 | |||
| rs41298006 | 0.925 | 0.080 | 22 | 19779119 | intron variant | G/A | snv | 5.9E-04 | 2 | ||
| rs12165908 | 1.000 | 0.040 | 22 | 19777658 | intron variant | G/C | snv | 0.20 | 1 | ||
| rs1329122220 | 1.000 | 0.080 | 22 | 19766433 | missense variant | C/A | snv | 2.4E-05 | 1 | ||
| rs1445910672 | 1.000 | 0.080 | 22 | 19761255 | stop gained | G/A;T | snv | 1 | |||
| rs1555895466 | 1.000 | 0.200 | 22 | 19761162 | stop gained | A/T | snv | 1 | |||
| rs1555896474 | 1.000 | 22 | 19765900 | splice acceptor variant | A/G | snv | 1 | ||||
| rs41297816 | 1.000 | 0.040 | 22 | 19776455 | intron variant | A/G | snv | 0.28 | 1 | ||
| rs41298838 | 1.000 | 0.200 | 22 | 19765921 | missense variant | G/A;T | snv | 5.2E-03 | 1 | ||
| rs74315522 | 1.000 | 0.200 | 22 | 19764224 | missense variant | C/G | snv | 1 |